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The palladium-catalyzed reaction of (hetero)aryl bromides, chlorides, and nonaflates with α-allyl-β-ketoesters provides ready efficient access to functionalized 2,3-dihydrofurans. The reaction tolerates several useful substituents including chloro, fluoro, ether, ketone, ester, cyano, and nitro groups. © The Royal Society of Chemistry 2011.

Cacchi, S., Fabrizi, G., Goggiamani, A., Iazzetti, A., Madec, D., Poli, G., Prestat, G., Functionalized 2,3-dihydrofurans via palladium-catalyzed oxyarylation of α-allyl-β-ketoesters, <<ORGANIC & BIOMOLECULAR CHEMISTRY>>, 2011; 9 (24): 8233-8236. [doi:10.1039/c1ob06593a] [http://hdl.handle.net/10807/200796]

Functionalized 2,3-dihydrofurans via palladium-catalyzed oxyarylation of α-allyl-β-ketoesters

Iazzetti, Antonia;
2011

Abstract

The palladium-catalyzed reaction of (hetero)aryl bromides, chlorides, and nonaflates with α-allyl-β-ketoesters provides ready efficient access to functionalized 2,3-dihydrofurans. The reaction tolerates several useful substituents including chloro, fluoro, ether, ketone, ester, cyano, and nitro groups. © The Royal Society of Chemistry 2011.
2011
Inglese
Cacchi, S., Fabrizi, G., Goggiamani, A., Iazzetti, A., Madec, D., Poli, G., Prestat, G., Functionalized 2,3-dihydrofurans via palladium-catalyzed oxyarylation of α-allyl-β-ketoesters, <<ORGANIC & BIOMOLECULAR CHEMISTRY>>, 2011; 9 (24): 8233-8236. [doi:10.1039/c1ob06593a] [http://hdl.handle.net/10807/200796]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10807/200796
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